A molecular phylogeny of the circum-Antarctic Opiliones family Neopilionidae

2021 ◽  
Author(s):  
Gonzalo Giribet ◽  
Kate Sheridan ◽  
Caitlin M. Baker ◽  
Christina J. Painting ◽  
Gregory I. Holwell ◽  
...  

The Opiliones family Neopilionidae is restricted to the terranes of the former temperate Gondwana: South America, Africa, Australia, New Caledonia and New Zealand. Despite decades of morphological study of this unique fauna, it has been difficult reconciling the classic species of the group (some described over a century ago) with recent cladistic morphological work and previous molecular work. Here we attempted to investigate the pattern and timing of diversification of Neopilionidae by sampling across the distribution range of the family and sequencing three markers commonly used in Sanger-based approaches (18S rRNA, 28S rRNA and cytochrome-c oxidase subunit I). We recovered a well-supported and stable clade including Ballarra (an Australian ballarrine) and the Enantiobuninae from South America, Australia, New Caledonia and New Zealand, but excluding Vibone (a ballarrine from South Africa). We further found a division between West and East Gondwana, with the South American Thrasychirus/Thrasychiroides always being sister group to an Australian–Zealandian (i.e. Australia + New Zealand + New Caledonia) clade. Resolution of the Australian–Zealandian taxa was analysis-dependent, but some analyses found Martensopsalis, from New Caledonia, as the sister group to an Australian–New Zealand clade. Likewise, the species from New Zealand formed a clade in some analyses, but Mangatangi often came out as a separate lineage from the remaining species. However, the Australian taxa never constituted a monophyletic group, with Ballarra always segregating from the remaining Australian species, which in turn constituted 1–3 clades, depending on the analysis. Our results identify several generic inconsistencies, including the possibility of Thrasychiroides nested within Thrasychirus, Forsteropsalis being paraphyletic with respect to Pantopsalis, and multiple lineages of Megalopsalis in Australia. In addition, the New Zealand Megalopsalis need generic reassignment: Megalopsalis triascuta will require its own genus and M. turneri is here transferred to Forsteropsalis, as Forsteropsalis turneri (Marples, 1944), comb. nov.

2002 ◽  
Vol 16 (6) ◽  
pp. 957 ◽  
Author(s):  
J. T. Jennings ◽  
A. D. Austin

This study examines the phylogeny, taxonomy, distribution and biology of the gasteruptiid subfamily Hyptiogastrinae and, at the same time, presents an overview of the family. Following a cladistic analysis of 35 discrete morphological characters, two monophyletic genera are recognised, Hyptiogaster Kieffer and Pseudofoenus s. l. Kieffer. As a consequence, the genera Aulacofoenus Kieffer, Crassifoenus Crosskey, and Eufoenus Szépligeti are synonymised with Pseudofoenus. A total of 88 species are recognised for the subfamily, 10 species of Hyptiogaster, which are restricted to mainland Australia, and 78 species of Pseudofoenus, 40 of which are described as new. Pseudofoenus has a restricted Gondwanan distribution and is found in Australia including Tasmania (65 spp.), New Guinea and New Britain (5 spp.), the south-west Pacific (New Caledonia, New Hebrides and Fiji – 2 spp.), New Zealand (4 spp.) and South America (2 spp.). No new species have been recorded from either New Zealand or South America. For Pseudofoenus, information on the distribution of each species, their biology (if known) and an identification key are presented.Following a taxonomic revision, the following new species are described: P. baileyi, sp. nov., P. baitetaensis, sp. nov., P. beverlyae, sp. nov., P. caperatus, sp. nov., P. cardaleae, sp. nov., P. carrabinensis, sp. nov., P. claireae, sp. nov., P. collessi, sp. nov., P. coorowensis, sp. nov., P. crosskeyi, sp. nov., P. douglasorum, sp. nov., P. eliseae, sp. nov., P. ericae, sp. nov., P. eustonensis, sp. nov., P. feckneri, sp. nov., P. gressitti, sp. nov., P. gullanae, sp. nov., P. hackeri, sp. nov., P. imbricatus, sp. nov., P. iqbali, sp. nov., P. kadowi, sp. nov., P. karimuiensis, sp. nov., P. kelleri, sp. nov., P. leinsterensis, sp. nov., P. macdonaldi, sp. nov., P. malkini, sp. nov., P. marshalli, sp. nov., P. masneri, sp. nov., P. mitchellae, sp. nov., P. morganensis, sp. nov., P. nalbarraensis, sp. nov., P. pumilis, sp. nov., P. schmidti, sp. nov., P. stevensi, sp. nov., P. tasmaniensis, sp. nov., P. taylori, sp. nov., P. umboiensis, sp. nov., P. walkeri, sp. nov. and P. zborowskii, sp. nov. The synonymy of Aulacofoenus, Crassifoenus and Eufoenus with Pseudofoenus result in the following new combinations: from Aulacofoenus: P. bungeyi (Jennings & Austin), comb. nov., P. deletangi (Schletterer), comb. nov., P. fallax (Schletterer), comb. nov., P. fletcheri (Jennings & Austin), comb. nov., P. goonooensis (Jennings & Austin), comb. nov., P. infumatus (Schletterer), comb. nov., P. kurmondi (Jennings & Austin), comb. nov., P. loxleyi (Jennings & Austin), comb. nov., P. marionae (Jennings & Austin), comb. nov., P. perenjorii (Jennings & Austin), comb. nov., P. swani (Jennings & Austin), comb. nov., P. thoracicus (Guérin Menéville), comb. nov., P. whiani (Jennings & Austin), comb. nov. and P. wubinensis (Jennings & Austin), comb. nov.; from Crassifoenus: P. houstoni (Jennings & Austin), comb. nov., P. grossitarsis (Kieffer), comb. nov and P. macronyx (Schletterer), comb. nov.; and from Eufoenus: P. antennalis (Schletterer), comb. nov., P. australis (Westwood), comb. nov., P. crassitarsis (Kieffer), comb. nov., P. darwini (Westwood), comb. nov., P. extraneus (Turner), comb. nov., P. ferrugineus (Crosskey), comb. nov., P. floricolus (Turner), comb. nov., P. inaequalis (Turner), comb. nov., P. melanopleurus (Crosskey), comb. nov., P. minimus (Turner), comb. nov., P. nitidiusculus (Turner), comb. nov., P. patellatus (Westwood), comb. nov., P. pilosus (Kieffer), comb. nov., P. reticulatus (Crosskey), comb. nov., P. rieki (Crosskey), comb. nov., P. ritae (Cheesman), comb. nov. and P. spinitarsis (Westwood), comb. nov. Pseudofoenus microcephalus (Crosskey), comb. nov. is transferred from Hyptiogaster and Eufoenus flavinervis (Kieffer) remains incertae sedis.


1978 ◽  
Vol 26 (4) ◽  
pp. 841
Author(s):  
RJ Raven

Two new genera, Plesiothele and Bymainiella, are erected to receive all the Australian species of the subfamily Hexathelinae, which now comprises four genera, including Hexathele with 20 species from New Zealand, and Scotinoecus with two species from South America. Plesiothele is a monotypic Tasmanian genus, type-species Hexathele fentoni Hickman, 1936. Bymainiella comprises 12 new species: B. boycei, B. boydi, B. brindabella, B. cannoni, B. grayi, B. lugubris, B. monteithi, B. montisbossi, B. otwayensis, B. polesoni, B. tubrabucca and B. variabilis; also B. montana (Hickman, 1927), and B. terraereginae (Raven, 1976), the latter being the type-species. The typespecies of Scotinoecus, S. cinereopilosus, is redescribed, and keys to the genera of the subfamily Hexathelinae, and to the Bymainiella species, are given. Two new indices are introduced to overcome the problem of bilateral variability. Bymainiella is believed to be the sister group of Scotinoecus.


2021 ◽  
Author(s):  
Anna A. Namyatova ◽  
Michael D. Schwartz ◽  
Gerasimos Cassis

The Lygus-complex is one of the most taxonomically challenging groups of Miridae (Heteroptera), and its Australian fauna is poorly studied. Here we examine the Australian taxa of the Lygus-complex using morphological and molecular methods. After a detailed morphological study of the material collected throughout Australia, Taylorilygus nebulosus is transferred to Diomocoris, with the genus recorded for the first time in this country. Taylorilygus apicalis, also widely distributed in Australia, is redescribed on the basis of Australian material. The genus Micromimetus is recorded for the first time in Australia, with M. celiae, sp. nov., M. hannahae, sp. nov., M. nikolai, sp. nov. and M. shofneri, sp. nov. described as new to science. Micromimetus pictipes is redescribed and its distributional range is increased. The monophyly of the Lygus-complex and relationships within this group were tested using cytochrome c oxidase subunit I (COI), 16S rRNA, 18S rRNA and 28S rRNA markers. The Lygus-complex has been found to be non-monophyletic. Phylogeny confirmed the monophyly of Micromimetus, and it has shown that Taylorilygus apicalis is closer to Micromimetus species than to Diomocoris nebulosus. This study is the initial step in understanding the Lygus-complex phylogeny; analyses with more taxa, more genes and morphology are needed to reveal the interrelationships within this group, and sister-group relationships of Australian taxa. http://zoobank.org/urn:lsid:zoobank.org:pub:7393D96B-2BBA-438D-A134-D372EFE7FB9E


2020 ◽  
Author(s):  
Gustavo Hormiga ◽  
Nikolaj Scharff

This paper addresses the systematics of the New Zealand spiders of the family Malkaridae. Malkarids are small araneoid spiders that live primarily in the leaf litter and mosses of temperate and tropical wet forests in Australia and New Zealand, with the exception of a single species in southern South America and another in New Caledonia. We treat the New Zealand species of Malkaridae that are not members of the subfamily Pararchaeinae, a monophyletic group of 11 new species that we classify in 2 new genera (Tingotingo, gen. nov. and Whakamoke, gen. nov.) and a new subfamily (Tingotinginae, subfam. nov.). We describe, diagnose, illustrate and map the distribution of specimen records of these 11 new species of New Zealand Malkaridae: Tingotingo porotiti, sp. nov., T. pouaru, sp. nov., T. tokorera, sp. nov., T. aho, sp. nov., Whakamoke orongorongo, sp. nov.; W. tarakina, sp. nov.; W. guacamole, sp. nov.; W. hunahuna, sp. nov.; W. paoka, sp. nov.; W. heru, sp. nov.; and W. rakiura, sp. nov. We also treat the phylogenetic relationships of Malkaridae and use the results of our previous work on the molecular phylogeny of Araneoidea as the bases for the classification of the family. Tingotingo, gen. nov. and Whakamoke, gen. nov. are sister clades. Tingotinginae, subfam. nov. is the sister group of the Malkarinae plus Pararchaeinae clade. We further hypothesise and discuss the morphological synapomorphies of Malkaridae, Tingotinginae, subfam. nov. and the two new genera.


2012 ◽  
Vol 43 (3-4) ◽  
pp. 175-212 ◽  
Author(s):  
Jakob Damgaard ◽  
Felipe Ferraz Figueiredo Moreira ◽  
Masakazu Hayashi ◽  
Tom A. Weir ◽  
Herbert Zettel

The phylogenetic relationships among selected species and genera of Mesoveliidae (Insecta: Hemiptera: Heteroptera: Gerromorpha) were investigated in a parsimony analysis of 2858 bp of DNA sequence data from the genes encoding COI + II, 16S rRNA and 28S rRNA. The resulting phylogeny showed that Mesoveloidea williamsiHungerford, 1929, from the subfamily Madeoveliinae, was sister group to Mniovelia Andersen & J.T. Polhemus, 1980, from the Mesoveliinae, thus making the latter subfamily paraphyletic. The genus MesoveliaMulsant & Rey, 1852 also showed to be paraphyletic, since an undescribed Laotian relative of M. indicaHorváth, 1915 and M. ujhelyiiLundblad, 1933 resulted as sister group to PhrynoveliaHorváth, 1915; and M. amoenaUhler, 1894 was sister species to Speovelia maritimaEsaki, 1929. Whereas these relationships were poorly or moderately supported, the remaining species of Mesovelia formed two distinct and well-supported clades, one comprising M. horvathiLundblad, 1933, M. hackeriHarris & Drake, 1941, and two undescribed species from Nigeria and New Caledonia, and another comprising M. vittigeraHorváth, 1895, M. stysi J.T. Polhemus & D.A. Polhemus, 2000, M. ebbenielseniAndersen & Weir, 2004, M. furcata Mulsant & Rey, 1952, and M. mulsantiWhite, 1879. A large genetic difference was found between populations of M. vittigera from Europe and Africa on one side and populations from Australia and New Caledonia on the other. DNA sequence data from a Japanese “M. vittigera” obtained from GenBank placed the specimen as strongly supported sister group to a Danish specimen of M. furcata. Comparisons of the 28S rRNA sequence data between the two specimens revealed a single C/T transition, while comparison with a Chinese female of M. furcata revealed one A/G and one C/T transition, thus suggesting mislabelling of the Japanese specimen, or an unrecognized presence of M. furcata in Japan. Considerable genetic differentiation was found between specimens of M. horvathi from Australia, New Caledonia, New Guinea, and Laos, and between sympatric specimens of M. mulsanti from Honduras, thus supporting earlier ideas of species-complexes in these two clades. Samples of Austrovelia caledonicaMalipatil & Monteith, 1983 from New Caledonia and Mniovelia kuscheli Andersen & J.T. Polhemus, 1980 from New Zealand’s North Island also revealed considerable intraspecific divergences indicating genetic isolation among geographically separated populations on these ancient islands.


2020 ◽  
Vol 34 (1) ◽  
pp. 1
Author(s):  
James K. Liebherr

The carabid beetle tribe Moriomorphini attains a disjunct austral geographical distribution, with member taxa occupying Australia, New Zealand, New Caledonia, the Sundas, southern South America and Polynesia. The group arose in Australia, the area exhibiting the greatest generic diversity for the tribe. In this contribution, two new genera are added to the Australian fauna. Pharetis thayerae, gen. nov., sp. nov., is described from Grenvillia, New South Wales, and Spherita newtoni, gen. nov., sp. nov., is described from Avon Valley National Park, Western Australia. Their phylogenetic placement within the tribe is accomplished by parsimony analysis based on 208 morphological characters across 124 taxa, 114 in-group species and 10 outgroup taxa representing Trechini, Psydrini and Patrobini. Nearly all polytypic moriomorphine genera are represented in the analysis by at least two exemplars, allowing initial tests of generic monophyly. A revised classification is proposed for Moriomorphini, with subtribal clades related as (Amblytelina + (Moriomorphina + Tropopterina)). The Western Australian genus Spherita is placed as adelphotaxon to Sitaphe Moore, a genus restricted to tropical montane Queensland. From the phylogenetic analysis, other non-contemporaneous east–west Australian disjunctions can be inferred, as well as multiple trans-Tasman area relationships between eastern Australia and New Zealand, all proposed to be of Miocene age. Pharetis exhibits a disjunct, trans-Antarctic relationship with Tropopterus Solier, its sister-group, distributed in southern South America. Alternative vicariance-based and dispersal-based hypotheses are discussed for the origin of Tropopterus. A review of the taxonomic development of the tribe illustrates the signal importance of monotypic genera in elucidating biological diversity.


1987 ◽  
Vol 1 (2) ◽  
pp. 201 ◽  
Author(s):  
ES Nielsen

The recently described primitive monotrysian heteroneuran moth family Palaephatidae was first discovered from southern South America and is here reported from Australia. The Australian palaephatid fauna consists of one endemic genus, Azaleodes Turner, with one named species, micronipha Turner, and three species here described as new: fuscipes, brachyceros and megaceros. All Australian species are very similar and it has not been possible to separate the females. The males possess an impressive array of hairpencils and pockets with specialised scales on wings and abdomen. One possible additional autapomorphy for the Palaephatidae is listed. The monophyly and systematic position of Azaleodes are discussed; it is concluded that Azaleodes is not the sister-group of the remaining, South American Palaephatidae but is monophyletic with Sesommata Davis and Metaphatus Davis.


2021 ◽  
Author(s):  
Daria M. Kupaeva ◽  
Tatiana S. Lebedeva ◽  
Tatiana P. Ashurkova ◽  
Andrey A. Prudkovsky ◽  
Daniel Vanwalleghem ◽  
...  

The life-cycle and polyp morphology of Margelopsidae representatives are very different from all other Aplanulata cnidarians. Until recently, their evolutionary origin and phylogenetic position has been a subject of significant speculation. A recent molecular study based only on COI data unexpectedly placed Margelopsidae as a sister group to all Aplanulata, despite the Margelopsid morphology suggests affiliation with Tubulariidae or Corymorphidae. Here we used multigene analyses, including nuclear (18S rRNA and 28S rRNA) and mitochondrial (16S rRNA and COI) markers of the Margelopsidae hydroid Margelopsis haeckelii Hartlaub, 1897, to resolve its phylogenetic position with respect to other hydrozoans. Our data provides strong evidence that M. haeckelii is a member of the family Corymorphydae, making the family Margelopsidae invalid. Furthermore, we show that medusa previously known as M. harlaubii Browne, 1903 is sister to Plotocnide borealis, Wagner, 1885 and might be a member of Boreohydridae. The phylogenetic signal of polyp and medusа stages is discussed in light of concept of inconsistent evolution and molecular phylogenetic analysis.


Author(s):  

Abstract A new distribution map is provided for Alternaria passiflorae Simmonds. Dothideomycetes: Pleosporales: Pleosporaceae. Host: passionflower (Passiflora sp.). Information is given on the geographical distribution in Asia (Bhutan, China, Guangdong, India, Kerala, Sikkim, West Bengal), Africa (Kenya, Malawi, Mauritius, South Africa, Tanzania, Uganda, Zambia, Zimbabwe), North America (Canada, British Columbia, Florida, Hawaii), South America (Brazil, Sao Paulo, Colombia, Venezuela), Oceania (Australia, Queensland, Western Australia, Fiji, New Caledonia, New Zealand, Niue, Norfolk Island, Papua New Guinea, Tonga).


2004 ◽  
Vol 18 (3) ◽  
pp. 235 ◽  
Author(s):  
Gregory D. Edgecombe ◽  
Gonzalo Giribet

Species assigned to the anopsobiine centipede genera Anopsobius Silvestri, 1899, and Dichelobius Attems, 1911, are widely distributed on fragments of the Gondwanan supercontinent, including temperate and tropical Australia, New Zealand, New Caledonia, the Cape region of South Africa, and southern South America. Phylogenetic relationships between Australasian and other Gondwanan Anopsobiinae are inferred based on parsimony and maximum likelihood analyses (via direct optimisation) of sequence data for five markers: nuclear ribosomal 18S rRNA and 28S rRNA, mitochondrial ribosomal 12S rRNA and 16S RNA, and the mitochondrial protein-coding cytochrome c oxidase subunit I. New molecular data are added for Anopsobius from South Africa and New Zealand, Dichelobius from New Caledonia, and a new species from Queensland, Australia, Dichelobius etnaensis, sp. nov. The new species is based on distinctive morphological and molecular data. The molecular phylogenies indicate that antennal segmentation in the Anopsobiinae is a more reliable taxonomic character than is spiracle distribution. The former character divides the Gondwanan clade into a 17-segmented group (Dichelobius) and a 15-segmented group (Anopsobius). Confinement of the spiracles to segments 3, 10 and 12 has at least two origins in the Gondwanan clade. The area cladogram for Dichelobius (Queensland (Western Australia + New Caledonia)) suggests a relictual distribution pruned by extinction.


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